Genomic Map
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Target Gene Details
Entrez Gene ID: | 81502 |
Gene Name: | histocompatibility minor 13 |
Gene Aliases: |
H13, IMP1, IMPAS, IMPAS-1, MSTP086, PSENL3, PSL3, SPP, SPPL1 |
Location: |
Chr.20:31514410-31569567 on Build GRCh38 |
Assay Gene Location: | Within Exon 1 |
| Gene Symbol | Transcript Accession | Exon Location | Assay Transcript Location | Protein ID |
|---|---|---|---|---|
| HM13 | NM_030789.3 | 1 | 136 | NP_110416.1 |
| NM_178580.2 | 1 | 136 | NP_848695.1 | |
| NM_178581.2 | 1 | 136 | NP_848696.1 | |
| NM_178582.2 | 1 | 136 | NP_848697.1 | |
| AF172086.1 | 1 | 87 | AAQ13609.1 | |
| AF483215.1 | 1 | 82 | AAM22076.1 | |
| AF515663.1 | AAN77099.1 | |||
| AJ345029.1 | 1 | 79 | CAC87790.1 | |
| AJ420895.1 | CAD13132.1 | |||
| AK074686.1 | BAC11138.1 | |||
| AK075283.1 | 1 | 96 | BAC11519.1 | |
| AK314410.1 | 1 | 104 | ||
| AY169310.1 | 1 | 93 | AAO12535.1 | |
| AY169311.1 | 1 | 93 | AAO12536.1 | |
| AY169312.1 | 1 | 93 | AAO12537.1 | |
| BC008938.2 | 1 | 107 | AAH08938.1 | |
| BC008959.2 | 1 | 107 | AAH08959.1 | |
| BC062595.1 | 1 | 87 | AAH62595.1 | |
| BI192962.1 | 1 | 109 | ||
| BI552780.1 | 1 | 121 | ||
| DA087240.1 | 1 | 136 | ||
| DQ168450.1 | 1 | 88 | ||
| HY026569.1 | 1 | 146 | ||
| KU178790.1 | ||||
| KU178791.1 |
Target Copy Number Variation Details
DGV Version: |
Release date: 2016-05-15, GRCh GRCh38 |
| Target Variation |
Location | CNV Subtype |
Genes |
|---|---|---|---|
| nsv470546 | Chr.20:31245806 - 31647499 on Build GRCh38 | Gain |
 HM13-AS1
DEFB117
DEFB119
DEFB123
DEFB124
HM13
REM1
MIR3193
DEFB118
DEFB116
ID1
DEFB115
DEFB121
LOC107985416
LINC00028
DEFB122
COX4I2
|
| dgv4300n100 | Chr.20:31247234 - 32033468 on Build GRCh38 | Gain |
HM13-AS1
TTLL9
ABALON
FOXS1
DEFB115
DEFB121
LOC107985416
DUSP15
DEFB122
DEFB117
TPX2
CCM2L
MYLK2
PDRG1
DEFB119
DEFB123
DEFB124
HM13
REM1
MIR3193
DEFB118
BCL2L1
DEFB116
ID1
XKR7
LINC00028
COX4I2
|
| esv2763228 | Chr.20:31247246 - 31651719 on Build GRCh38 | Gain |
HM13-AS1
DEFB117
DEFB119
DEFB123
DEFB124
HM13
REM1
MIR3193
DEFB118
DEFB116
ID1
DEFB115
DEFB121
LOC107985416
LINC00028
DEFB122
COX4I2
|
| esv3645652 | Chr.20:31500710 - 31576564 on Build GRCh38 | Gain |
HM13-AS1
LOC107985416
HM13
|
| nsv585911 | Chr.20:31305698 - 31688103 on Build GRCh38 | Gain |
HM13-AS1
DEFB117
DEFB119
DEFB123
DEFB124
HM13
REM1
MIR3193
DEFB118
BCL2L1
DEFB116
ID1
DEFB121
LOC107985416
LINC00028
DEFB122
COX4I2
|
Back To TopMore Information
Set Membership: |
Intragenic
Exonic
DGV Variation
|
Panther Classification:
Gene Ontology Categories:
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